# Ab Ardent

- Location (FDA's records): Tonawanda, NY
- FDA decisions: 13 (1998–2013): 13 510(k) clearances
- Product codes: EBF (6), EJJ (5), KLE (1), EMA (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ivoclar Vivadent, Inc.: 1 (https://510kreport.com/company/ivoclar-vivadent)

## Recent decisions
- K131753: Meridian (Nov 14, 2013)
- K040465: Latit Flow (Jul 20, 2004)
- K022971: Microhybrid 11 (Nov 25, 2002)
- K022973: Adhesive 14 (Nov 22, 2002)
- K022972: Microfill 13 (Nov 22, 2002)
- K022975: Etching 15 (Nov 22, 2002)
- K022974: Microhybrid 12 (Nov 22, 2002)
- K020452: High Silver Conventional (May 7, 2002)

Source page: https://510kreport.com/company/ab-ardent